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3-V Bioscience-2640

Phase 1

Metabolic Syndrome | Small molecule | Metabolic |Sagimet Biosciences Inc. - Series A|Trials Updated: May 4, 2025

3-V Bioscience-2640 development status

Highest phase Phase 1
Registered trials 1 across 1 sponsor since Oct 2001

Success Probability

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Market & Valuation

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Trial Design

UNCONTROLLEDDMC
Total Trials1
Total Enrollment12

FDA Designations

No designations recorded

3-V Bioscience-2640 clinical trials

3-V Bioscience-2640 · 1 trial · 1 indication

Phase 1 1
NCT02948569Evaluation of 3-V Bioscience-2640 to Reduce de Novo Lipogenesis in Subjects With Characteristics of Metabolic SyndromeMetabolic Syndrome
COMPLETED12 Analytics
PHASE1COMPLETED
Evaluation of 3-V Bioscience-2640 to Reduce de Novo Lipogenesis in Subjects With Characteristics of Metabolic Syndrome
Metabolic SyndromeUnlock trial analytics

Study Endpoints

Primary Endpoints

Change in Hepatic Lipogenesis
Baseline and after 10 days of treatment

Subject undergoes a stable isotope infusion followed by blood draws. Plasma lipid samples are measured by gas chromatography/mass spectrophotometry.

Secondary Endpoints

Change in Liver Fat Measured by MRI
Baseline and 10 days of treatment
Change in Skin Sebum Production
Baseline and 10 days of treatment
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Study Design & Arms

AllocationNA
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
3-V Bioscience-2640EXPERIMENTALSubjects will take a singly daily dose of 3-V Bioscience-2640 before bedtime or 22:30, whichever comes first, for 10 days.

Interventions

NameTypeDescription
3-V Bioscience-2640DRUGSubjects will take a singly daily dose of 3-V Bioscience-26400 before bedtime or 22:30, whichever comes first, for 10 days.
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Eligibility Criteria

Age Range35 Years to 60 Years
SexMALE
Healthy VolunteersNo
Study Sites1

Inclusion Criteria: 1. Men with characteristics of metabolic syndrome 1. Waist circumference greater than 40 in (102 cm) 2. Plasma TG greater than 150 mg/dL 3. HDL cholesterol less than 40 mg/dL 4. Blood pressure greater than or equal to 130/85 mmHg 5. Fasting plasma glucose greater...

Countries:United States
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Competitive Landscape -Metabolic Syndrome 28 trials

Top 3 of 6 competitors

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Frequently asked questions about 3-V Bioscience-2640

What is 3-V Bioscience-2640?

3-V Bioscience-2640 is an investigational small molecule developed by Sagimet Biosciences Inc. for metabolic syndrome. It was studied in a Phase 1 clinical trial evaluating its ability to reduce de novo lipogenesis in subjects with characteristics of metabolic syndrome. The drug has completed one Phase 1 trial and is not approved for any indication.

What is 3-V Bioscience-2640 used for?

3-V Bioscience-2640 was studied for metabolic syndrome, specifically to evaluate its effect on reducing de novo lipogenesis in subjects with characteristics of the condition. The research was conducted in a Phase 1 trial that has been completed. It is an investigational therapy and has not been approved for use in metabolic syndrome or any other indication.

Who makes 3-V Bioscience-2640?

3-V Bioscience-2640 is being developed by Sagimet Biosciences Inc., which trades under the ticker SGMT. The company is responsible for the clinical development of this investigational small molecule for metabolic syndrome.

What phase is 3-V Bioscience-2640 in?

3-V Bioscience-2640 is in Phase 1 clinical development. One Phase 1 trial has been completed, and there are currently no active trials. The drug remains investigational and has not received FDA approval for any indication.

What clinical trials is 3-V Bioscience-2640 in?

3-V Bioscience-2640 has been evaluated in one completed Phase 1 clinical trial, NCT02948569, titled "Evaluation of 3-V Bioscience-2640 to Reduce de Novo Lipogenesis in Subjects With Characteristics of Metabolic Syndrome." The trial enrolled 12 participants in the United States and studied males aged 35 years and older.